Anaesthesia and non-obstetric surgery in pregnancy
Neither the core nor intermediate curriculum explicitly mention knowledge of this topic, choosing to dance euphemistically around it with items such as:
"explains why anaesthetic techniques must be modified in the pregnant patient" and "explains the potential impact of anaesthetic technique on patient outcome" .
Nevertheless, this topic has appeared as either SAQ or CRQ on four occasions in the past ten years; 2014 (33% pass rate), 2016 (58%), 2019 (32%) and most recently in 2022 (50%).
The examiners reports, aside from lamenting generally poor answers, consistently make reference to a lack of knowledge on risks to the foetus and steps in reducing these.
A recent BJA Education article on the topic raises suspicion of the question reappearing in a CRQ soon...
Approximately 1 - 2% of pregnant women require non-obstetric surgery during their pregnancy
Challenges arise from a need to simultaneously:
Ensure the safety of the parturient
Consider foetal wellbeing and minimise foetal risk
Account for the physiological, anatomical and pharmacological changes associated with pregnancy
Indications
Common indications for non-obstetric surgery in pregnancy
Appendicitis
Cholecystitis
Trauma
Malignancy
For other gynaecological disease
Timing of non-obstetric surgery in pregnancy
First trimester - 45%
Second trimester - 35%
Third trimester - 20%
Outcomes following surgery in pregnancy
Peri-operative maternal outcomes for general abdominal, pelvic and trauma surgery are similar to those of non-pregnant women
The rate of 30-day mortality and overall morbidity is not different between pregnant and non-pregnant women undergoing the same surgery
Studies support use of a laparoscopic approach with inflation pressure <15mmHg as it is associated with fewer materno-foetal complications
Common maternal complications include:
Reoperation (3.6%)
Infection (2%) or other wound-associated morbidity (1.4%)
Prolonged mechanical ventilation or need for re-intubation (2.0%)
VTE (0.5%)
Death (0.25%)
Foetal risks arise from:
The disease process itself
Intra-operative disturbances to uteroplacental blood flow i.e. maternal hypoxia/hypotension
Anaesthetic drugs
All modern anaesthetic agents at clinical doses are not reported to be teratogenic
Inadequate evidence base to establish effects of anaesthesia on neurodevelopment, but using regional techniques and reducing duration of GA is advised
Surgery
Said risks include:
Foetal Risk
Notes
Foetal loss
Risk of spontaneous miscarriage during the 1st trimester (10.5%) or overall (5.8%) is 3x higher than parturients not undergoing surgery
Pre-term labour
50% higher than patients who aren't undergoing surgery in pregnancy Risk increases as the pregnancy progresses
Need for LSCS
Higher
Low birth weight
Higher incidence
Effects of GA on pregnancy
Exposure to anaesthesia may adversely affect neurodevelopment in the foetus, therefore:
Elective surgery is contraindicated in pregnancy
Elective surgery should be delayed until at least 6 weeks post-partum
If surgery cannot be delayed until after delivery, the 2nd trimester (13 - 28 weeks) may be the optimal timing
Effects by gestational age
Gestation
Effect
<2 weeks
'All or nothing' i.e. no effect or pregnancy will be lost
3 - 8 weeks
Anaesthesia is best avoided as organogenesis is taking place
>8 weeks
Risk of growth retardation, premature delivery/labour and foetal loss
>28 weeks (3rd trimester)
Risk of precipitating premature labour
The disease process
Acute infectious or inflammatory illnesses requiring surgery can induce pre-term labour due to increased uterine irritability via:
The disease process itself
Maternal pyrexia
Surgical handling of uterus intra-operatively, intentional or not
The proposed surgery and whether regional techniques might be suitable
The seniority of the team; ideally senior surgeon and senior anaesthetist
Stage of pregnancy and its physiological effects
Choice of anaesthetic drugs and foetal impact (see below)
Effects of anaesthetic drugs on pregnancy
Propofol
Does not alter uterine blood flow but decreases perinatal survival, so manufacturer advises against use in pregnancy
Often used as first line induction agent for pregnant patients due to familiarity amongst anaesthetists
Thiopentone
In animal studies is teratogenic in high doses
Causes reduced uteroplacental blood flow (up to 35%) due to cardio-depressant effect and reduced SVR
Increased risk of AAGA in pregnant patients undergoing GA LSCS using thiopentone
Ketamine
Can increase uterine tone and therefore reduce uteroplacental blood flow, so should be avoided
Are non-teratogenic
The drugs do not (readily) cross the placenta due to being bulky, water-soluble, charged molecules
There may be prolonged duration of action (except atracurium) due to:
Alterations in hepatic metabolism of aminosteroid agents
Acquired pseudocholinesterase deficiency affecting suxamethonium
Of note, sugammadex is not recommended for routine reversal of neuromuscular block in pregnancy
It can encapsulate progesterone and potentially disrupt the integrity of the pregnancy
Nitrous oxide
Teratogenic in rats if used at high concentration for prolonged periods
As such is felt to be safe for use in humans due to short time periods and as Entonox
Volatile agents
Potential teratogenicity in animals
Effects in pregnant humans unclear; sevoflurane or isoflurane recommended if use is required
Cause relaxation of the gravid uterus and are therefore not likely to cause pre-term labour
NB MAC is reduced by the effect of progesterone
Paracetamol is not known to be harmful in pregnancy
Opioids are considered safe in pregnancy at appropriate doses
NSAIDs are contraindicated
May cause closure of the ductus arteriosus in utero and persistent pulmonary HTN of the new-born
Amide local anaesthetics are not teratogenic but can increase uterine tone so should be avoided
Perioperative management of the parturient undergoing non-obstetric surgery during pregnancy
Pre-operative
Standard anaesthetic pre-assessment, though naturally comes with an obstetric twist
Perform essential investigations only
Ensure adequate VTE prophylaxis
Standard fasting rules apply
Routine antacid/prokinetic prophylaxis from 12 - 14 weeks gestation due to delayed gastric emptying, relaxed LOS and reflux risk
Some suggestion this is overkill and an individualised approach may be preferable
Assess foetal wellbeing with ultrasound and CTG; document foetal heart rate
Intra-operative
AAGBI as standard
Arterial line may facilitate better steadying of the haemodynamic ship
Foetal monitoring if practicable, although CTG may look abnormal under GA and requires specialist interpretation
Use regional technique wherever possible
Moderate and deep sedation have both been used safely in pregnancy
LMA relatively contraindicated from 12 weeks onwards due to delayed gastric emptying
RSI technique relatively indicated due to higher aspiration risk (although evidence base would suggest this may not be as great as is described)
Be mindful of higher incidence of difficult airway and hypoxaemia from reduced FRC
Left lateral tilt from 18 - 20 weeks to mitigate effects of aortocaval compression
Maintain normal physiology as much as possible (obviousy)
Maintain uteroplacental blood flow by avoiding hypoxia or deranged CO2
Minimise uterine handling
Ensure adequate intra-operative VTE prophylaxis
Post-operative
Foetal heart rate monitoring
Ongoing lateral tilt
Analgesia: paracetamol + opioids + regional technique ± local anaesthetic wound infiltration
VTE prophylaxis